Canonical Allele Identifier: CA2367752745
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs2090191475

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763198G>A , CM000682.2:g.48763198G>A GRCh38
NC_000020.10:g.47379735G>A , CM000682.1:g.47379735G>A GRCh37
NC_000020.9:g.46813142G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15318C>T MANE Select ENSP00000361009.3:n.220-15318C>T
ENST00000371941.3:c.220-15318C>T ENSP00000361009.3:n.220-15318C>T
NM_020820.3:c.220-15318C>T NP_065871.2:n.220-15318C>T
NM_020820.4:c.220-15318C>T MANE Select NP_065871.3:n.220-15318C>T